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The safety of orthokeratology contact lens wear in slowing the axial elongation of the eye in children.
Santodomingo-Rubido, Jacinto; Cheung, Sin-Wan; Villa-Collar, César.
Afiliação
  • Santodomingo-Rubido J; Global R&D, Menicon Co., Ltd, Nagoya, Japan. Electronic address: j.santodomingo@menicon.com.
  • Cheung SW; School of Optometry, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
  • Villa-Collar C; Faculty of Biomedical and Health Sciences, Universidad Europea, Madrid, Spain.
Cont Lens Anterior Eye ; : 102258, 2024 Jul 12.
Article em En | MEDLINE | ID: mdl-39003152
ABSTRACT

PURPOSE:

To evaluate the safety of orthokeratology contact lens wear in slowing the axial elongation of the eye in myopic children.

METHODS:

Safety data from three prospective studies, which evaluated the use of orthokeratology for slowing myopia progression in children in comparison to a parallel control group of single-vision spectacle lens wearers over a 2-year period, were pooled together for analysis. The primary and secondary safety endpoints are the comparisons of adverse events and slit-lamp findings grades ≥ 2 between orthokeratology and control groups, respectively.

RESULTS:

Collectively, data from 125 orthokeratology and 118 control subjects were analyzed in this study. Of these, 101 (81 %) and 88 (75 %) orthokeratology and control subjects completed the 2-year follow-up period, respectively. Nineteen orthokeratology subjects experienced 28 adverse events, of which 6 were significant, whereas just one adverse event was found in the control group; this difference was statistically significant (p < 0.001). Most adverse events found in the orthokeratology group were corneal in nature, primarily corneal abrasion/staining, accounting for around 40 % of all adverse events. Of the 28 adverse events, only 18 (3 significant) are likely to be contact lens-related, leading to incidence rates of total and device-related adverse events per 100 patient years of lens wear (95 % confidence intervals) of 13.1 (9.2-18.2) and 8.4 (5.4-10.7), respectively. No significant differences were found between groups in the total number of silt-lamps findings with grades ≥ 2 (p > 0.05).

CONCLUSION:

Around 13% of eyes wearing overnight orthokeratology contact lenses are likely to experience an adverse event over one year of lens wear, with this figure being lower when considering device-related adverse events alone. No serious adverse events were found, with most being non-significant. These results inform eye care practitioners on the safety of orthokeratology lenses when prescribed for slowing myopia progression to myopic children.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cont Lens Anterior Eye Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cont Lens Anterior Eye Ano de publicação: 2024 Tipo de documento: Article
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